FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES

K Number: K052062 · Decision Aug 25, 2005
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
36
Review Days
27

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Basic Information

Device Name
ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
K Number
K052062
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alliance Medical Corp.
Date Received
July 29, 2005
Decision Date
August 25, 2005
Product Code
KTT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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K Number Device Name
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K060091 ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES
K053316 REPROCESSED COMPRESSION SLEEVES
K052918 REPROCESSED EXTERNAL FIXATION DEVICES
K052603 REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS
K052414 REPROCESSED ELECTROPHYSIOLOGY CATHETER
K052064 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
K052065 ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Search all 36 clearances from Alliance Medical Corp. →